International Medical Device Conferences

A list of international medical device conferences, medical device meetings and medical device training courses for the medical device industry and in vitro diagnostic medical device industry.

To add your event to this list, please click here.

DATE	TITLE	LOCATION	ORGANISER
August 2010
4	Applying Process Capability Analysis to ISO 13485	Webinar	ComplianceOnline +1 650 620 3915
6	Reducing Ethylene Oxide (EO) Sterilisation costs while maintaining regulatory compliance	Webinar	ComplianceOnline +1 650 620 3915
9	Gamma Steriliser Validation: Method 1 and VDmax25 per ISO 11137	Webinar	ComplianceOnline +1 650 620 3915
12	Supplier Evaluation and Assessment Program: How to meet FDA QSR and ISO 13485 requirements in a cost effective manner	Webinar	ComplianceOnline +1 650 620 3915
12	Principles and Practices of Traceability and Calibration	Webinar	ComplianceOnline +1 650 620 3915
17	Troubleshooting ethylene oxide (EO) processes	Webinar	ComplianceOnline +1 650 620 3915
24	Recalls of Medical Devices in the US	Webinar	ComplianceOnline +1 650 620 3915
24	Software Verification and Validation Planning	Webinar	ComplianceOnline +1 650 620 3915
26	Document Approval, Control, and Distribution: How to Meet FDA QSR and ISO 13485 Requirements in a Relatively Paper-Free Manner	Webinar	ComplianceOnline +1 650 620 3915
27	How to Manage a Medical Device Recall Efficiently and Effectively	Webinar	ComplianceOnline +1 650 620 3915
30	Understanding International Standards for Medical Devices	Webinar	ComplianceOnline +1 650 620 3915
31	Product Risk Management - ISO 14971 and ICH Q9	Webinar	ComplianceOnline +1 650 620 3915

DATE	TITLE	LOCATION	ORGANISER
September 2010
9	Controlling Change to meet GMP Requirements	Webinar	ComplianceOnline +1 650 620 3915
14	Developing an ethylene oxide (EO) sterilisation process for a product with limitations	Webinar	ComplianceOnline +1 650 620 3915
15	Market Access for Medical Devices	Webinar	Kakushin Group +421 2207 14599
16	Medical Devices in the EU: the CE Mark and Directive 93/42/EEC	Webinar	ComplianceOnline +1 650 620 3915
16-18	The Pan African Health Expo and Conference 2010	South Africa	Fair Consultants SA +27 21 713 3360
21	Medical Device Changes and The 510(k)	Webinar	ComplianceOnline +1 650 620 3915
21-23	Medical Technology Vigilance, Post-Market Surveillance (PMS) and Risk Management	Cranfield University, UK	Cranfield University +44 (0)1234 754192
22-23	MEDTEC Ireland	Galway, Ireland	Canon Communications +353 1 8060557
27	Medical Device and Diagnostics Summit on Regulatory Approvals	Boston, MA, USA	CBI +1 800 817 8601
27-28	FDA Approval Process for Medical Devices	London, UK	Management Forum Ltd +44 (0)1483 730071
28	Validating Radiation Sterilization for medical device industries	Webinar	ComplianceOnline +1 650 620 3915
29	FDA Requirements for Combination Products	London, UK	Management Forum Ltd +44 (0)1483 730071
30-1 Oct	Medical Device & Diagnostics Corporate Compliance & Ethics Conference	Chicago, IL, USA	Q1 Productions +1 312 822 8100

DATE	TITLE	LOCATION	ORGANISER
October 2010
1-30 Nov	Regulatory Affairs Certification exam window	Worldwide	Regulatory Affairs Professionals Society (RAPS) +1 301 770 2920, ext 245
11	Technical File Documentation and Review	London, UK	Management Forum Ltd +44 (0)1483 730071
12	Supplier Management for Medical Devices and IVDs	London, UK	Management Forum Ltd +44 (0)1483 730071
12-13	Good Manufacturing Practice	London, UK	Informa Life Sciences +44 (0)20 7017 7481
13	Risk Management and Risk Analysis - A Core Compliance Process	London, UK	Management Forum Ltd +44 (0)1483 730071
14	Managing Medical Device Software Projects - Is Your Software a Medical Device and is it Correctly Classified?	London, UK	Management Forum Ltd +44 (0)1483 730071
18-19	Regulatory Affairs for Medical Devices	London, UK	PTI Europe +44 (0)20 7017 7481
18-19	Biological Evaluation of Medical Devices	London, UK	Management Forum Ltd +44 (0)1483 730071
18-20	AdvaMed 2010: The MedTech Conference	Washington, DC, USA	AdvaMed +1 202 434 7213
19-20	Clinical Evaluations & Investigations for Medical Devices	Berlin, Germany	IQPC +44 (0) 20 7368 9300
20	Gamma Sterilizer Validation: Method 1 and VDmax25 per ISO 11137	Webinar	ComplianceOnline +1 650 620 3915
20-21	Labelling and Packaging for Medical Devices and IVDs Conference	London, UK	Informa Life Sciences +44 (0)20 7017 7481
20-21	Drug/Device and Device/Drug Combinations in the EU	London, UK	Management Forum Ltd +44 (0)1483 730071
24-27	2010 RAPS Annual Conference & Exhibition	San Jose, CA, USA	Regulatory Affairs Professionals Society (RAPS) +1 301 770 2920
25-26	Point of Care Diagnostics - Market Adoption and Technology Trends	London, UK	SMi Group Ltd +44 (0)20 7827 6722

DATE	TITLE	LOCATION	ORGANISER
November 2010
18-19	Regulatory Affairs for Combination Products	London, UK	PTI Europe +44 (0)20 7017 7481
18-19	Medical Devices Directives: Lessons Learned and the Way Forward	Brussels, Belgium	Regulatory Affairs Professionals Society (RAPS) +1 301 770 2920
23-24	Drug Device Combination Products	Brussels, Belgium	Informa Life Sciences +44 (0)20 7017 7481

DATE	TITLE	LOCATION	ORGANISER
December 2010
1-2	Medical Device and IVD Regulation in the Americas	London, UK	Informa Life Sciences +44 (0)20 7017 7481
9-10	FDA Inspections for Medical Devices	London, UK	Management Forum Ltd +44 (0)1483 730071

DATE	TITLE	LOCATION	ORGANISER
February 2011
8-10	HuLST Expo Human Life Science Test Expo	Cologne, Germany	Total World Media +44 1306 803030
11-12	Conference On Indian Medical Devices & Plastics Disposables Industry 2011	Ahmedabad, India	Medical Plastics Data Service +91 79 26740611